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1CLQ

CRYSTAL STRUCTURE OF A REPLICATION FORK DNA POLYMERASE EDITING COMPLEX AT 2.7 A RESOLUTION

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsCHESS BEAMLINE A1
Synchrotron siteCHESS
BeamlineA1
Temperature [K]100
Detector technologyCCD
Collection date1998-10-15
DetectorADSC
Spacegroup nameH 3
Unit cell lengths209.740, 209.740, 114.250
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution40.000 - 2.700
R-factor0.23
Rwork0.230
R-free0.28400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1waj
RMSD bond length0.008
RMSD bond angle1.400
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 Overall
Low resolution limit [Å]40.000
High resolution limit [Å]2.700
Rmerge0.080

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Total number of observations51455

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Number of reflections23329

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<I/σ(I)>18.1
Completeness [%]97.2
Redundancy2.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.512

*

12% (W/V) PEG 350MME, 150 MM CACL2, 100 MM SODIUM CACODYLATE, PH 6.5, 12 DEGREES C, VAPOR DIFFUSION, HANGING DROP, temperature 285K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111PEG
211CACL2
311SODIUM CACODYLATE
412PEG
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirmPEG35012 (%(w/v))
21reservoircalcium chloride150 (mM)
31reservoirsodium cacodylate100 (mM)

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